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Behr, Meckenzie
18
results:
Search for persons
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Format
Online (18)
Mediatypes
Articles (Online) (7)
OpenAccess-fulltext (11)
Sorted by: Relevance
Sorted by: Year
?
1
Molecular diagnosis and novel genes and phenotypes in a ped..:
Strong, Alanna
;
Behr, Meckenzie
;
Lott, Carina
...
Scientific Reports. 13 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1038/..
?
2
Attitudes among Parents towards Return of Disease-Related P..:
Terek, Shannon
;
Del Rosario, Maya C.
;
Hain, Heather S.
...
Journal of Personalized Medicine. 12 (2022) 12 - p. 1945 , 2022
Link:
https://doi.org/10.3390/..
?
3
Rare copy number variants in over 100,000 European ancestry..:
Li, Yun Rose
;
Glessner, Joseph T.
;
Coe, Bradley P.
...
Nature Communications. 11 (2020) 1 - p. , 2020
Link:
https://doi.org/10.1038/..
?
4
Harmonizing Clinical Sequencing and Interpretation for the ..:
Zouk, Hana
;
Venner, Eric
;
Lennon, Niall J.
...
The American Journal of Human Genetics. 105 (2019) 3 - p. 588-605 , 2019
Link:
https://doi.org/10.1016/..
?
5
Ethical Considerations Related to Return of Results from Ge..:
Fossey, Robyn
;
Kochan, David
;
Winkler, Erin
...
Journal of Personalized Medicine. 8 (2018) 1 - p. 2 , 2018
Link:
https://doi.org/10.3390/..
?
6
The Philadelphia Neurodevelopmental Cohort: A publicly avai..:
Satterthwaite, Theodore D.
;
Connolly, John J.
;
Ruparel, Kosha
...
NeuroImage. 124 (2016) - p. 1115-1119 , 2016
Link:
https://doi.org/10.1016/..
?
7
The Philadelphia Neurodevelopmental Cohort: constructing a ..:
Calkins, Monica E.
;
Merikangas, Kathleen R.
;
Moore, Tyler M.
...
Journal of Child Psychology and Psychiatry. 56 (2015) 12 - p. 1356-1369 , 2015
Link:
https://doi.org/10.1111/..
?
8
Molecular diagnosis and novel genes and phenotypes in a ped..:
Strong, Alanna
;
Behr, Meckenzie
;
Lott, Carina
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9849333/. , 2023
Link:
http://www.ncbi.nlm.nih...
?
9
Rare copy number variants in over 100,000 European ancestry..:
Li, Yun Rose
;
Glessner, Joseph T
;
Coe, Bradley P
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6959272/. , 2020
Link:
http://www.ncbi.nlm.nih...
?
10
Rare copy number variants in over 100,000 European ancestry..:
Li, Yun Rose
;
Glessner, Joseph T
;
Coe, Bradley P
...
info:eu-repo/semantics/altIdentifier/pmid/31937769. , 2020
Link:
http://hdl.handle.net/11..
?
11
The Philadelphia Neurodevelopmental Cohort: constructing a ..:
Calkins, Monica E
;
Merikangas, Kathleen R
;
Moore, Tyler M
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4598260/. , 2015
Link:
http://www.ncbi.nlm.nih...
?
12
The Philadelphia Neurodevelopmental Cohort: A Publicly Avai..:
Satterthwaite, Theodore D
;
Connolly, John J
;
Ruparel, Kosha
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4591095/. , 2015
Link:
http://www.ncbi.nlm.nih...
?
13
Molecular diagnosis and novel genes and phenotypes in a ped..:
Alanna Strong
;
Meckenzie Behr
;
Carina Lott
...
https://doi.org/10.1038/s41598-023-27641-0. , 2023
Link:
https://doi.org/10.1038/..
?
14
Attitudes among Parents towards Return of Disease-Related P..:
Shannon Terek
;
Maya C. Del Rosario
;
Heather S. Hain
...
https://www.mdpi.com/2075-4426/12/12/1945. , 2022
Link:
https://doi.org/10.3390/..
?
15
Attitudes among Parents towards Return of Disease-Related P..:
Shannon Terek
;
Maya C. Del Rosario
;
Heather S. Hain
...
https://dx.doi.org/10.3390/jpm12121945. , 2022
Link:
https://doi.org/10.3390/..
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